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• W2023563304 abstract "We developed two-photon scanning patterned illumination microscopy (2P-SPIM) for super-resolution two-photon imaging. Our approach used a traditional two-photon microscopy setup with temporally modulated excitation to create patterned illumination fields. Combing nine different illuminations and structured illumination reconstruction, super-resolution imaging was achieved in two-photon microscopy. Using 2P-SPIM we achieved a lateral resolution of 141 nm, which represents an improvement by a factor of 1.9 over the corresponding diffraction limit. We further demonstrated super-resolution cellular imaging by 2P-SPIM to image actin cytoskeleton in mammalian cells and three-dimensional imaging in highly scattering retinal tissue." @default.
• W2023563304 created "2016-06-24" @default.
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• W2023563304 date "2015-04-07" @default.
• W2023563304 modified "2023-10-18" @default.
• W2023563304 title "Super-resolution two-photon microscopy via scanning patterned illumination" @default.
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• W2023563304 doi "https://doi.org/10.1103/physreve.91.042703" @default.
• W2023563304 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4565794" @default.
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